Variant report

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs1006810	0.95[ASN][1000 genomes]
rs11620188	0.93[AFR][1000 genomes];0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1322385	0.85[ASN][1000 genomes]
rs1590277	0.93[ASN][1000 genomes]
rs2077255	0.86[ASN][1000 genomes]
rs326524	0.81[EUR][1000 genomes]
rs6490346	0.86[ASN][1000 genomes]
rs68008399	0.91[ASN][1000 genomes]
rs7317087	0.85[ASN][1000 genomes]
rs7326464	0.86[ASN][1000 genomes]
rs7328602	0.86[ASN][1000 genomes]
rs7332330	0.86[ASN][1000 genomes]
rs7334030	0.85[ASN][1000 genomes]
rs7337190	0.86[ASN][1000 genomes]
rs7339409	0.85[ASN][1000 genomes]
rs745423	0.86[ASN][1000 genomes]
rs754395	0.86[ASN][1000 genomes]
rs7986144	0.85[ASN][1000 genomes]
rs7994068	0.84[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs913494	0.86[ASN][1000 genomes]
rs9314927	0.84[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs9506080	0.83[AFR][1000 genomes];0.81[AMR][1000 genomes];0.84[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9506087	0.93[ASN][1000 genomes]
rs9508235	0.86[ASN][1000 genomes]
rs9508236	0.86[ASN][1000 genomes]
rs9508238	0.81[AFR][1000 genomes];0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9508239	0.84[ASN][1000 genomes]
rs9550435	0.81[AFR][1000 genomes];0.80[AMR][1000 genomes];0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9550436	0.93[ASN][1000 genomes]
rs9550437	0.93[ASN][1000 genomes]
rs9551598	0.93[ASN][1000 genomes]
rs9551599	0.93[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv533835	chr13:29141132-29962069	Weak transcription Strong transcription Flanking Active TSS Bivalent/Poised TSS Enhancers Genic enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
2	esv3406145	chr13:29616606-29917459	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:29606200-29623600	Weak transcription	Aorta	Aorta
2	chr13:29612400-29633600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr13:29619200-29623200	Enhancers	Fetal Heart	heart

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